Variant #0000566268 (NC_000019.9:g.13428086C>T, NM_001127221.1:c.1398G>A (CACNA1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13428086C>T
DNA change (hg38) g.13317272C>T
Published as CACNA1A(NM_023035.2):c.1398G>A (p.S466=)
ISCN -
DB-ID CACNA1A_000358
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 15:15:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

P-domain     
CACNA1A NM_001127221.1 -?/. - c.1398G>A - r.(?) p.(Ser466=) -
CACNA1A NM_023035.2 -?/. - c.1398G>A - r.(?) p.(Ser466=) -


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